Richard M Fleming PhD, MD, JD - DOCUMENTATION

md_a

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Messages
468

DOCUMENTATION​

The following diagram shows how SARS-CoV-2 is passed from person to person through respiratory droplets. Once inside the body the virus will invade our cells and reproduce itself. In response to the virus our immune system will attack the invader launching first a response from T-cells designed to kill the cells infected with the virus and later an antibody response designed to kill the virus before it gets into another cell.

This diagram also shows how too much of a good thing can cause harm to the body. When our VIRAL immune response, either because of other health problems we have (comorbidities) produce too much response OR because there is too much of the virus (e.g. vaccines) in our body; the outcome is INFLAMMATION and BLOOD CLOTTING (InflammoThrombotic Response – ITR) that can kill us (COVID-19).

The document numbers listed on the diagram below match the numbered documents providing links to the research as well as other materials not only explaining these issues but also the Gain-of-Function (GoF) research responsible for the development of this man-made virus.

SARS-CoV-2: Documents 17, 20.​

InflammoThrombotic Response (ITR): Documents 18, 19, 21, 33, 37, 49.​

Treatments: Document 40.​

Gain-of-Function (With HIV-gp120; PRRA & Prion-like Domain): Documents 7, 9, 14, 15, 16, 21, 22, 26, 35, 36, 38, 39, 41, 42, 43, 44, 45, 46, 47, 48, 50, 54, 56, 57.​

BIOWEAPON: 58, 59, 60, 61, 62.​

Vaccines: Documents 1, 2, 3, 13, 24, 31, 32, 51, 52, 53, 55, 56.​

Enters Nucleus with DNA: Documents 10, 11, 12, 63, 64.​

Antibody Dependent Enhancement of Virus: Documents 4, 5, 6.​

Neurologic - Central Nervous System - Brain: 8, 23, 25, 27, 28, 29, 30, 34.​



1. EUA Requirements by FDA

October 2020



2. Pfizer EUA document

December 10, 2020



3. Moderna EUA Document

December 17, 2020



4. SARS-CoV-1 Antibody Dependent Enchancement (ADE)

July 5, 2011



5. ADE shown in animals including primates

January 2, 2021



6. ADE (Osaka Paper) showing antibodies to NTD increase infectivity of SARS-CoV-2

December 18, 2020



7. Prion-like Domains

March 29,, 2020



8. Amyloid Precursor Proteins and Neurologic Disease

May 21, 2019



9. Amyloidosis and Prion Diseases

October 26, 2010



10. SARS-CoV-2 RT back into human DNA

December 13, 2020



11. Platlets and LINE-1 to Generate RNA-DNA Hybrids with Reverse Transcriptase

April 2018



12. Reverse Transcription Produces Mechanism for Long Term Survival and Recurrent Infections

January 9, 2019



13. Pfizer vaccines contains 13 billion mRNA repetitions in the low dose of 30-micrograms.

December 25, 2020



14. Baric & Zhengli Shi re-engineer the HKU4 spike to increase Corona Virus Infectivity. Gain-of-Function (GoF)

September 2015



15. SARS-CoV-2 Gain-of-Function Hall of Shame

October 1, 2020



16. Evidence that SARS-CoV-2 is not naturally evolved

July 1, 2020



17. South African Mutation of SARS-CoV-2

December 22, 2020



18. InflammoThrombotic Response (ITR)

August 18,2020



19. Massive Blood Clots Kill COVID Patients

January 9, 2019



20. Cryo-Electron Tomography of SARS-CoV-2 showing spike proteins

October 9, 2020



21. PRRA Superantigen increases inflammation

October 13, 2020



22. PRRA Insert essential for infection of human lung cells and brain

May 1, 2020



23. SARS-CoV-2 Spike protein crosses the blood brain barrier in mice study

December 16, 2020



24. Neurological adverse events associated with vaccines

June 2002



25. SARS-CoV-2 Invades Brain

November 30, 2020



26. Neuropilin-1binds to Furin (PRRA) Cleavage site to increase Infectivity.

November 13, 2020



27. Spike Protein Crosses BBB to Infect Brain

November 30, 2020



28. Fatal Invasion of Brain by SARS-CoV-2 Depends upon ACE2.

January 15, 2021



29. SARS-CoV-2 Interferes With Recognition of the Severity of Hypoxemia.

July 28, 2020



30. RNA can Behave like Prions.

July 1, 2020



31. Influenza mRNA Spreads Throughout Body and Found in Lungs, Brain, Heart for 14-days.

October 1995



32. Moderna mRNA Vaccine for Influenza Spreads Throughout Body.

March 24, 2017



33. How Immune Cells Cross the Blood-Brain Barrier.

February 4, 2019



34. Neuroinvasion, Encephalitis and Neuron Death with SARS-CoV-2.

January 19, 2021



35. Jean claude Perez § Luc Montagnier - COVID-19, SARS and Bats Coronaviruses Genomes Unexpected Exogenous RNA Sequences

May 29, 2020



36. Jean claude Perez § Luc Montagnier - COVID-19, COVID-19, SARS and Bats Coronaviruses Genomes Peculiar Homologous RNA Sequences

July 7, 2020



37. Autopsy Findings of InflammoThrombotic Response (ITR) in Patients with COVID-19

JAugust 18, 2020



38. TMPRSS2 and Furin Both Essential for SARS-CoV-2 Infection of Cells.

July 23, 2020



39. Protein structure and sequence re-analysis of 2019-nCoV genome does not indicate snakes as its intermediate host or the unique similarity between its spike protein insertions and HIV-1

March 22, 2020



40. Treatment of SARS-CoV-2 & COVID-19.

February 8, 2021​




41. Evidence of Gain-of-Function.

September 14, 2020



42. Gain-of-Function Hall of Shame.

October 1, 2020



43. Origins of SARS-CoV-2.

February 7, 2021



44. Genetic Structure of SARS-CoV-2.

October 16, 2020​




45. Origins of SARS and PRRA.

August 12, 2020



46. The Corona Conspiracy.

October 2020



47. Probabilities of SARS-CoV-2 Origin.

November 12, 2020



48. The Fauci COVID-19 Dossier.

February 18, 2021



49. Primate studies show Inflammation in Brain & Lewy Bodies.

February 23, 2021



50. Patent for PRRA Furin Cleavage Site with Certain Patent Rights Owned by U.S. Governmnent (NIH).

May 29, 2007



51. Janssen (Johnson & Johnson) EUA Document.

February 26, 2021



52. Ad26 [J & J]Prior Studies Reveal Only Temporary Immunity.

July 18, 2012



53. The Coxsackie & Adenovirus Receptor (CAR).

June 8, 1999



54. Deleted Wuhan Databases.​

February 23, 2021



55. CDC Document on Adenovirus Vaccines.​

January 8, 2020



56. COVID-19 Vaccines and Brain Injury.​

April 10, 2021



57. SARS-CoV-2 Accelerates Amyloid Formation.​

April 12, 2021



58. SARS-CoV-2 Is an Unrestricted Bioweapon.​

Released April 24, 2021



59. SARS-CoV-2 is a Sophisticated Lab Modification.​

Released April 24, 2021



60. CNN Lies and Misinformation.​

September 14, 2020



61. SARS-CoV-2 - A Scientific Discussion of Lab Origin.​

March 25, 2021



62. Lethal Deception.​

April 22, 2021



63. Reverse Transcription of SARS-CoV-2 in Human Cells.​

March 29, 2021



64. Evidence in Support of SARS-CoV-2 (Viral)-Human Cell Chimers.​

March 29, 2021


 
Last edited:

Lollipop2

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Amazing collection of resources and data. Surprised no one responded. So much evidence here.
 

Vileplume

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This connects to an email Peat recently sent me, where he seemed to liken the vaccine shedding effect to the effects of the virus itself. Peat said “ Most people aren’t harmed by the corona virus, so the similar material coming from vaccinated people is likely to be equally harmless,” which implies that the amount of the virus we’d get via ingestion from shedding would not be the “too much” that you mention in your second paragraph. It would be a smaller amount, which would at least not make our bodies spike protein factories, like the direct injection of the vaccine could.
 

Old Irenaeus

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1,127
This connects to an email Peat recently sent me, where he seemed to liken the vaccine shedding effect to the effects of the virus itself. Peat said “ Most people aren’t harmed by the corona virus, so the similar material coming from vaccinated people is likely to be equally harmless,” which implies that the amount of the virus we’d get via ingestion from shedding would not be the “too much” that you mention in your second paragraph. It would be a smaller amount, which would at least not make our bodies spike protein factories, like the direct injection of the vaccine could.
I love that quote from Peat.
 

J.R.K

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Aug 4, 2020
Messages
1,837
Thank you so much @md_a I appreciate you putting all this together for us, especially when so much of this information is being deleted as of late.

DOCUMENTATION​

The following diagram shows how SARS-CoV-2 is passed from person to person through respiratory droplets. Once inside the body the virus will invade our cells and reproduce itself. In response to the virus our immune system will attack the invader launching first a response from T-cells designed to kill the cells infected with the virus and later an antibody response designed to kill the virus before it gets into another cell.

This diagram also shows how too much of a good thing can cause harm to the body. When our VIRAL immune response, either because of other health problems we have (comorbidities) produce too much response OR because there is too much of the virus (e.g. vaccines) in our body; the outcome is INFLAMMATION and BLOOD CLOTTING (InflammoThrombotic Response – ITR) that can kill us (COVID-19).

The document numbers listed on the diagram below match the numbered documents providing links to the research as well as other materials not only explaining these issues but also the Gain-of-Function (GoF) research responsible for the development of this man-made virus.

SARS-CoV-2: Documents 17, 20.​

InflammoThrombotic Response (ITR): Documents 18, 19, 21, 33, 37, 49.​

Treatments: Document 40.​

Gain-of-Function (With HIV-gp120; PRRA & Prion-like Domain): Documents 7, 9, 14, 15, 16, 21, 22, 26, 35, 36, 38, 39, 41, 42, 43, 44, 45, 46, 47, 48, 50, 54, 56, 57.​

BIOWEAPON: 58, 59, 60, 61, 62.​

Vaccines: Documents 1, 2, 3, 13, 24, 31, 32, 51, 52, 53, 55, 56.​

Enters Nucleus with DNA: Documents 10, 11, 12, 63, 64.​

Antibody Dependent Enhancement of Virus: Documents 4, 5, 6.​

Neurologic - Central Nervous System - Brain: 8, 23, 25, 27, 28, 29, 30, 34.​



1. EUA Requirements by FDA

October 2020



2. Pfizer EUA document

December 10, 2020



3. Moderna EUA Document

December 17, 2020



4. SARS-CoV-1 Antibody Dependent Enchancement (ADE)

July 5, 2011



5. ADE shown in animals including primates

January 2, 2021



6. ADE (Osaka Paper) showing antibodies to NTD increase infectivity of SARS-CoV-2

December 18, 2020



7. Prion-like Domains

March 29,, 2020



8. Amyloid Precursor Proteins and Neurologic Disease

May 21, 2019



9. Amyloidosis and Prion Diseases

October 26, 2010



10. SARS-CoV-2 RT back into human DNA

December 13, 2020



11. Platlets and LINE-1 to Generate RNA-DNA Hybrids with Reverse Transcriptase

April 2018



12. Reverse Transcription Produces Mechanism for Long Term Survival and Recurrent Infections

January 9, 2019



13. Pfizer vaccines contains 13 billion mRNA repetitions in the low dose of 30-micrograms.

December 25, 2020



14. Baric & Zhengli Shi re-engineer the HKU4 spike to increase Corona Virus Infectivity. Gain-of-Function (GoF)

September 2015



15. SARS-CoV-2 Gain-of-Function Hall of Shame

October 1, 2020



16. Evidence that SARS-CoV-2 is not naturally evolved

July 1, 2020



17. South African Mutation of SARS-CoV-2

December 22, 2020



18. InflammoThrombotic Response (ITR)

August 18,2020



19. Massive Blood Clots Kill COVID Patients

January 9, 2019



20. Cryo-Electron Tomography of SARS-CoV-2 showing spike proteins

October 9, 2020



21. PRRA Superantigen increases inflammation

October 13, 2020



22. PRRA Insert essential for infection of human lung cells and brain

May 1, 2020



23. SARS-CoV-2 Spike protein crosses the blood brain barrier in mice study

December 16, 2020



24. Neurological adverse events associated with vaccines

June 2002



25. SARS-CoV-2 Invades Brain

November 30, 2020



26. Neuropilin-1binds to Furin (PRRA) Cleavage site to increase Infectivity.

November 13, 2020



27. Spike Protein Crosses BBB to Infect Brain

November 30, 2020



28. Fatal Invasion of Brain by SARS-CoV-2 Depends upon ACE2.

January 15, 2021



29. SARS-CoV-2 Interferes With Recognition of the Severity of Hypoxemia.

July 28, 2020



30. RNA can Behave like Prions.

July 1, 2020



31. Influenza mRNA Spreads Throughout Body and Found in Lungs, Brain, Heart for 14-days.

October 1995



32. Moderna mRNA Vaccine for Influenza Spreads Throughout Body.

March 24, 2017



33. How Immune Cells Cross the Blood-Brain Barrier.

February 4, 2019



34. Neuroinvasion, Encephalitis and Neuron Death with SARS-CoV-2.

January 19, 2021



35. Jean claude Perez § Luc Montagnier - COVID-19, SARS and Bats Coronaviruses Genomes Unexpected Exogenous RNA Sequences

May 29, 2020



36. Jean claude Perez § Luc Montagnier - COVID-19, COVID-19, SARS and Bats Coronaviruses Genomes Peculiar Homologous RNA Sequences

July 7, 2020



37. Autopsy Findings of InflammoThrombotic Response (ITR) in Patients with COVID-19

JAugust 18, 2020



38. TMPRSS2 and Furin Both Essential for SARS-CoV-2 Infection of Cells.

July 23, 2020



39. Protein structure and sequence re-analysis of 2019-nCoV genome does not indicate snakes as its intermediate host or the unique similarity between its spike protein insertions and HIV-1

March 22, 2020



40. Treatment of SARS-CoV-2 & COVID-19.

February 8, 2021​




41. Evidence of Gain-of-Function.

September 14, 2020



42. Gain-of-Function Hall of Shame.

October 1, 2020



43. Origins of SARS-CoV-2.

February 7, 2021



44. Genetic Structure of SARS-CoV-2.

October 16, 2020​




45. Origins of SARS and PRRA.

August 12, 2020



46. The Corona Conspiracy.

October 2020



47. Probabilities of SARS-CoV-2 Origin.

November 12, 2020



48. The Fauci COVID-19 Dossier.

February 18, 2021



49. Primate studies show Inflammation in Brain & Lewy Bodies.

February 23, 2021



50. Patent for PRRA Furin Cleavage Site with Certain Patent Rights Owned by U.S. Governmnent (NIH).

May 29, 2007



51. Janssen (Johnson & Johnson) EUA Document.

February 26, 2021



52. Ad26 [J & J]Prior Studies Reveal Only Temporary Immunity.

July 18, 2012



53. The Coxsackie & Adenovirus Receptor (CAR).

June 8, 1999



54. Deleted Wuhan Databases.​

February 23, 2021



55. CDC Document on Adenovirus Vaccines.​

January 8, 2020



56. COVID-19 Vaccines and Brain Injury.​

April 10, 2021



57. SARS-CoV-2 Accelerates Amyloid Formation.​

April 12, 2021



58. SARS-CoV-2 Is an Unrestricted Bioweapon.​

Released April 24, 2021



59. SARS-CoV-2 is a Sophisticated Lab Modification.​

Released April 24, 2021



60. CNN Lies and Misinformation.​

September 14, 2020



61. SARS-CoV-2 - A Scientific Discussion of Lab Origin.​

March 25, 2021



62. Lethal Deception.​

April 22, 2021



63. Reverse Transcription of SARS-CoV-2 in Human Cells.​

March 29, 2021



64. Evidence in Support of SARS-CoV-2 (Viral)-Human Cell Chimers.​

March 29, 2021


 

Nemo

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Joined
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Messages
2,163
This connects to an email Peat recently sent me, where he seemed to liken the vaccine shedding effect to the effects of the virus itself. Peat said “ Most people aren’t harmed by the corona virus, so the similar material coming from vaccinated people is likely to be equally harmless,” which implies that the amount of the virus we’d get via ingestion from shedding would not be the “too much” that you mention in your second paragraph. It would be a smaller amount, which would at least not make our bodies spike protein factories, like the direct injection of the vaccine could.

I know everyone wants to be reassured. But we are not dealing with a natural virus. We are dealing with a bioweapon and it just keeps looking more and more like the vax is a bioweapon too. It may be foiled by Ivermectin but the people who put this out are really trying to hurt us.

The stuff coming from the vaxxes is tweaked to make it more like the South African and other more virulent strains.

It's a GMO spike protein, not the wild Covid spike protein we saw last year in the U.S.

The vax mRNA is designed to produce 100x as much spike protein and make it last a lot longer and be more susceptible to misfolding as in prion disease.

And the vax mRNA does other bad things. It kills your natural antibodies and reprograms your immune system to make those spike proteins last even longer. It tweaks the spike protein to hide better and look more like your endogenous proteins. Also, by knocking out everything but spike protein-specific antibodies, it increases the risk of ADE.

So the stuff coming from vaccinated people is not like the benign coronavirus we first saw in the U.S. in the wild. We saw with wild Covid that 10 virus particles could turn into full-blown disease in a vulnerable person. Again, the vax mRNA is designed to make 100x the spike protein that those 10 wild virus particles would make.

This is likely why we're seeing offices of people negatively impacted by a single employee getting the vax or by mere contact of people who interacted with health care workers who had handled the vaxxes.

I have a feeling Ray said this before seeing the latest research on what's in these vaxxes.
 
Last edited:

Nemo

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Messages
2,163
We need to get the word out: "Most people aren’t harmed by the corona virus."

We need to get the word out: "More people are hurt by the new mutations than 2020's coronavirus and the vaxxes are making the new mutations much more virulent. Also the vax spike proteins are worse than the ones from 2020's coronavirus."

When you have an office full of women develop bleeding problems after exposure to a vaxxed coworker, or a woman waking up covered in bruises after sleeping with her newly-vaxxed husband, you're seeing symptoms of immune thrombocytopenia via environmental transmission. That is the vax mRNA making a more virulent spike protein that is much harder for your cells to degrade.


p. 18 View of Worse Than the Disease? Reviewing Some Possible Unintended Consequences of the mRNA Vaccines Against COVID-19

And think about this. The nanoparticles from the vax make their way from their injection site in muscle to the nearest lymph node and then into every tissue in your body except the kidneys, including your brain (across the blood brain barrier) and your skin. They make it into your bone marrow.

You really think they aren't capable of traveling from the injection site through the skin and exhalation to other people?
 
Last edited:

Birdie

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@Nemo Yes, In one of the threads, you may recall, somebody, I don't recall who, posted a more recent response from Ray with 3 videos and some articles to read attached.
 

Drareg

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Thanks for this!

I posted about Ralph Baric, Peat mentioned him in a KMUD radio interview last year!
No spotlight on Baric from the MSM, his absence says everything.


 

Nemo

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Messages
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@Nemo Yes, In one of the threads, you may recall, somebody, I don't recall who, posted a more recent response from Ray with 3 videos and some articles to read attached.

That's right. Thank you, Birdie.
 

Birdie

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Under Documentation we have:

" This diagram also shows how too much of a good thing can cause harm to the body. When our VIRAL immune response, either because of other health problems we have (comorbidities) produce too much response OR because there is too much of the virus (e.g. vaccines) in our body; the outcome is INFLAMMATION and BLOOD CLOTTING (InflammoThrombotic Response – ITR) that can kill us (COVID-19)."

"Too much of the virus (e.g. vaccines) in our body;" But, I thought there was no virus in the vaccine, so do the vaccines cause viruses to multiply in the body?
 

Birdie

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I guess so.
 

J.R.K

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We need to get the word out: "More people are hurt by the new mutations than 2020's coronavirus and the vaxxes are making the new mutations much more virulent. Also the vax spike proteins are worse than the ones from 2020's coronavirus."

When you have an office full of women develop bleeding problems after exposure to a vaxxed coworker, or a woman waking up covered in bruises after sleeping with her newly-vaxxed husband, you're seeing symptoms of immune thrombocytopenia via environmental transmission. That is the vax mRNA making a more virulent spike protein that is much harder for your cells to degrade.


p. 18 View of Worse Than the Disease? Reviewing Some Possible Unintended Consequences of the mRNA Vaccines Against COVID-19

And think about this. The nanoparticles from the vax make their way from their injection site in muscle to the nearest lymph node and then into every tissue in your body except the kidneys, including your brain (across the blood brain barrier) and your skin. They make it into your bone marrow.

You really think they aren't capable of traveling from the injection site through the skin and exhalation to other people?
Terrifying stuff @Nemo! I agree that we need to get the word out but having a conversation with people on this topic well it is almost like you are one of those people that bring up their religion and then try to convert you ( maybe that is just my experience), so unless someone brings it up in a conversation I try to be the one that listens quietly. I am always amazed at how willing people are to take something that they have no idea of what is in it, the short, medium or long term side effects. I have four people whom I consider to be intelligent people, who have taken the vaccine for the first round, and have had small to medium reactions, one felt nauseous two weeks after last week, he went to the Doctor and he told him that it was his bad hip that he is waiting on a replacement for, so he shouldn’t work until after the surgery. He was doing fine up until then.
But I digress my point is that I typically end up saying,” what if only ten percent of what ,”the conspiracy theorists”, (myself included) are right and you just get an autoimmune disease, there is no redo on this, you will probably end up on Humira for $1500.00 per month for the rest of your life no biggie right?
Dr Tenpenny is right on one thing for sure, all of us who choose to remain in the control group (if there is one given the reactions between the vaccinated and unvaccinated), We all have to make some hard choices, ie no travel etc, but my belief is that if and when the side effects start, we may get some of those lost liberties back, time is the true test, we just need to wait. Andrew Lloyd Webber be damned for trying to guilt trip people into making a bad decision.
 

Giraffe

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Under Documentation we have:

" This diagram also shows how too much of a good thing can cause harm to the body. When our VIRAL immune response, either because of other health problems we have (comorbidities) produce too much response OR because there is too much of the virus (e.g. vaccines) in our body; the outcome is INFLAMMATION and BLOOD CLOTTING (InflammoThrombotic Response – ITR) that can kill us (COVID-19)."

"Too much of the virus (e.g. vaccines) in our body;" But, I thought there was no virus in the vaccine, so do the vaccines cause viruses to multiply in the body?
The spike protein causes blood clotting even without being part of a virus, and the vaccines are supposed to trick our cells to produce the spike protein.
 
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